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食品和饲料成分中沙门氏菌有效回收的预富集条件

Preenrichment Conditions for Effective Recovery of Salmonella in Foods and Feed Ingredients.

作者信息

D'Aoust J Y, Maishment C

机构信息

Bureau of Microbial Hazards, Health Protection Branch, Health and Welfare Canada, Tunney's Pasture, Ottawa, Ontario, Canada, K1A 0L2.

出版信息

J Food Prot. 1979 Feb;42(2):153-157. doi: 10.4315/0362-028X-42.2.153.

Abstract

The efficacy of Clausen, EE, Eugon, GN, Tergitol 7, lactose and nutrient broths as Salmonella preenrichment media was evaluated using 165 food samples with an incident contamination level ranging from 1.5 to 460 salmonellae/100 g. Replicate food samples (100 g) were preenriched in each of seven media (900 ml) for 6 h and 24 h at 35 C; various amounts (10, 1.0 and 0.1 ml) of preenriched cultures were selectively enriched in tetrathionate brilliant green (43 C) and selenite cystine (35 C) broths and plated on bismuth sulfite and brilliant green sulfa agars. Short (6 h) and 24-h preenrichment conditions resulted in 26 (16%) and 8 (5%) false negative results, respectively. Recovery of Salmonella from 6-h but not 24-h preenrichment cultures also varied directly with the portion of culture inoculated into selective enrichment broths. None of the preenrichment media tested performed satisfactorily at 6 h of incubation where levels of recovery ranged from 32 to 62%; at 24 h, good recovery was obtained with all media (95 to 100%) except EE broth (74%). The incidence of competitive flora was significantly higher on selenite + brilliant green sulfa than on tetrathionate + bismuth sulfite; transfer volumes (10 and 1.0 ml) and preenrichment media did not contribute significantly to the presence of non-salmonellae on plating media. Characteristics of preenrichment media were found to be less critical than preenrichment incubation time for effective recovery of Salmonella in foods and feed ingredients. The use of 1.0- rather than 10-ml preenrichment transfer volume is indicated because it proved to be completely reliable under our experimental conditions and reduced the cost of analyses.

摘要

使用165份食品样本评估了克劳森肉汤、EE肉汤、优贡肉汤、GN肉汤、特洁醇7、乳糖肉汤和营养肉汤作为沙门氏菌预增菌培养基的效果,这些食品样本的沙门氏菌污染水平为每100克1.5至460个。将重复的食品样本(100克)在七种培养基(900毫升)中的每一种中于35℃预增菌6小时和24小时;将不同量(10毫升、1.0毫升和0.1毫升)的预增菌培养物在四硫磺酸盐亮绿肉汤(43℃)和亚硒酸盐胱氨酸肉汤(35℃)中进行选择性增菌,并接种到亚硫酸铋和亮绿磺胺琼脂平板上。短时间(6小时)和24小时预增菌条件分别导致26例(16%)和8例(5%)假阴性结果。从6小时而非24小时预增菌培养物中回收沙门氏菌的情况也与接种到选择性增菌肉汤中的培养物比例直接相关。在培养6小时时,所测试的预增菌培养基均未表现出令人满意的效果,回收率在32%至62%之间;在24小时时,除EE肉汤(74%)外,所有培养基的回收率都很高(95%至100%)。亚硒酸盐 + 亮绿磺胺平板上竞争性菌群的发生率显著高于四硫磺酸盐 + 亚硫酸铋平板;转移体积(10毫升和1.0毫升)和预增菌培养基对平板培养基上非沙门氏菌的存在没有显著影响。发现预增菌培养基的特性对于有效回收食品和饲料成分中的沙门氏菌不如预增菌培养时间关键。建议使用1.0毫升而非10毫升的预增菌转移体积,因为在我们的实验条件下它被证明是完全可靠的,并且降低了分析成本。

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